chr19-43665358-C-T

Variant names:

• chr19-43665358-C-T
• rs184935465
• NM_002659.4:c.268G>A
• PLAUR p.Glu90Lys

GermlineCancer (beta)

Variant summary

Our verdict is Uncertain significance.

+1 Uncertain · Cold

-7

-6

-1

0

+5

+6

+9

+10

BenignB

Likely BenignLB

UncertainVUS

Likely PathogenicLP

PathogenicP

The variant received 1 classification points (ACGS-UK Somatic Oncogenicity v2025). O3_Supporting

The NM_002659.4(PLAUR):c.268G>A (p.Glu90Lys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The gene PLAUR is a tumor suppressor gene (CancerMine: 1 TSG, 2 oncogene, 4 driver citations). The gene PLAUR is a known oncogene (CancerMine: 1 TSG, 2 oncogene, 4 driver citations). The gene PLAUR is a cancer driver gene (CancerMine: 1 TSG, 2 oncogene, 4 driver citations). The variant allele was found at a cumulative frequency of 0.0000768 (AC=124) in the gnomAD database across 1,613,934 control chromosomes (no homozygotes observed). The grpmax filtering allele frequency (95% CI) is 0.0000839. Variant has been reported in ClinVar as Uncertain Significance (★). Other variants at the same amino acid position have been reported in ClinVar (not pathogenic): p.E90G: Uncertain_significance (ClinVar VariationId 2607848, 1 star) The variant has been observed in cBioPortal in 1 sample across 1 study and 1 cancer type; somatic enrichment level: NONE (Observed in at most one deduplicated cBioPortal case.).

• Frequency:
  • Genomes: 𝑓 0.000046 (0 hom., cov: 30)
  • Exomes 𝑓: 0.000080 (0 hom.)
• Consequence: PLAUR NM_002659.4 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 3.31
• Publications: 3 publications found

Genes affected

PLAUR (HGNC:9053): (plasminogen activator, urokinase receptor) This gene encodes the receptor for urokinase plasminogen activator and, given its role in localizing and promoting plasmin formation, likely influences many normal and pathological processes related to cell-surface plasminogen activation and localized degradation of the extracellular matrix. It binds both the proprotein and mature forms of urokinase plasminogen activator and permits the activation of the receptor-bound pro-enzyme by plasmin. The protein lacks transmembrane or cytoplasmic domains and may be anchored to the plasma membrane by a glycosyl-phosphatidylinositol (GPI) moiety following cleavage of the nascent polypeptide near its carboxy-terminus. However, a soluble protein is also produced in some cell types. Alternative splicing results in multiple transcript variants encoding different isoforms. The proprotein experiences several post-translational cleavage reactions that have not yet been fully defined. [provided by RefSeq, Jul 2008]

ENSG00000308028 (HGNC:):

Classification according to ACGS-UK Somatic Oncogenicity v2025

Classification was made for transcript:

Our verdict: Uncertain_significance. The variant received 1 points.

Apply	Criterion Code & Title / Strength	Strength	Rationale / Clinical Context
	O3Absent or very rare in population		Very rare in gnomAD (popmax AF <0.01%) — O3 supporting; GnomAD effective popmax AF = 0.000084 — very rare (O3 supporting [+1])

Variant Effect in Transcripts

Automated classification analysis was done for transcript: NM_002659.4. You can select a different transcript below to see updated classification assignments.

RefSeq Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	PLAUR NM_002659.4	MANE Select	c.268G>A p.Glu90Lys	missense	Exon 3 of 7	Prot: NP_002650.1 UniProt:
	PLAUR NM_001005377.3		c.268G>A p.Glu90Lys	missense	Exon 3 of 6	Prot: NP_001005377.1 UniProt:
	PLAUR NM_001301037.2		c.268G>A p.Glu90Lys	missense	Exon 3 of 6	Prot: NP_001287966.1 UniProt:

PLAUR NM_002659.4

MANE Select

HGVSc / HGVSpc.268G>Ap.Glu90Lys

Exon rankExon 3 of 7

missense

Prot: NP_002650.1UniProt: Q03405-1

PLAUR NM_001005377.3

HGVSc / HGVSpc.268G>Ap.Glu90Lys

Exon rankExon 3 of 6

missense

Prot: NP_001005377.1UniProt: Q03405-3

PLAUR NM_001301037.2

HGVSc / HGVSpc.268G>Ap.Glu90Lys

Exon rankExon 3 of 6

missense

Prot: NP_001287966.1UniProt: M0R1I2

Ensembl Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	PLAUR ENST00000340093.8	TSL:1MANE Select	c.268G>A p.Glu90Lys	missense	Exon 3 of 7	Prot: ENSP00000339328.3 UniProt:
	PLAUR ENST00000221264.8	TSL:1	c.268G>A p.Glu90Lys	missense	Exon 3 of 6	Prot: ENSP00000221264.3 UniProt:
	PLAUR ENST00000601723.5	TSL:1	c.268G>A p.Glu90Lys	missense	Exon 3 of 6	Prot: ENSP00000471881.1 UniProt:

PLAUR ENST00000340093.8

TSL:1MANE Select

HGVSc / HGVSpc.268G>Ap.Glu90Lys

Exon rankExon 3 of 7

missense

Prot: ENSP00000339328.3UniProt: Q03405-1

PLAUR ENST00000221264.8

TSL:1

HGVSc / HGVSpc.268G>Ap.Glu90Lys

Exon rankExon 3 of 6

missense

Prot: ENSP00000221264.3UniProt: Q03405-3

PLAUR ENST00000601723.5

TSL:1

HGVSc / HGVSpc.268G>Ap.Glu90Lys

Exon rankExon 3 of 6

missense

Prot: ENSP00000471881.1UniProt: M0R1I2

Frequencies

Allele frequencies (AF), counts (AC/AN), homozygotes and coverage

Common (AF > 0.05 / Hom > 5)

Rare (AF ≤ 0.0001 / Hom ≤ 1)

Source / population	AF	AC	Hom	AN	Coverage
Global population databases 6 sources Large-scale international reference populations
GnomAD3 genomes	AF: 0.0000461	AC:7	Hom:0	AN:151952	Cov:30
GnomAD2 exomes	AF: 0.0000398	AC:10	Hom:	AN:251486	Cov:
GnomAD4 exome	AF: 0.0000800	AC:117	Hom:0	AN:1461864	Cov:31
GnomAD4 genome	AF: 0.0000460	AC:7	Hom:0	AN:152070	Cov:30
TOPMed (Bravo)	AF: 0.0000340	AC:9	Hom:0	AN:264690	Cov:
ALFA (dbGaP/dbSNP Allele Frequency Aggregator)	AF: 0.0000550	AC:3	Hom:0	AN:54568	Cov:

Showing 6 sources

Case/control cohorts

Cohort	Cases			Controls
	AF	AC	AN	AF	AC	AN
BipEx(Bipolar disorder (including schizoaffective))	0.000106	3	28418	0.00	0	28844
Epi25(Epilepsy)	0.0000238	1	41958	0.0000598	4	66888
SCHEMA(Schizophrenia)	0.0000247	3	121546	0.0000368	7	190144

Showing 3 cohortsAllele count / allele number. AF is computed from the counts for ASC (not provided by the source).

ClinVar

ClinVar submissions

Significance: Uncertain significance

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	1	-	not specified (1)

Computational Scores

Algorithm	Calibrated pred.	Score	Prediction
AlphaGenome AVI	Pathogenic	33
AlphaMissense	Pathogenic	0.95
BayesDel_addAF	Benign	-0.079	T
BayesDel_noAF	Benign	-0.17
CADD	Uncertain	25
DANN	Uncertain	0.99
DEOGEN2	Benign	0.15	T
Eigen	Uncertain	0.20
Eigen_PC	Benign	0.023
FATHMM_MKL	Benign	0.52	D
FuncVEP CTI	Pathogenic	0.73
GPN-Star LLR	N/A	-5.8
GPN-Star score	N/A	5.8
LIST_S2	Uncertain	0.89	D
M_CAP	Uncertain	0.29	D
MetaRNN	Benign	0.40	T
MetaSVM	Benign	-0.48	T
Mutation Taster	N/A	80/20	polymorphism
MutationAssessor	Benign	1.8	L
PhyloP100	Benign	3.3
popEVE	Benign	-3.6
PrimateAI	Uncertain	0.57	T
PROVEAN	Uncertain	-3.0	D
RBP_binding_hub_radar	N/A	0.0
RBP_regulation_power_radar	N/A	2.1
REVEL	Uncertain	0.52
Sift	Uncertain	0.0040	D
Sift4G	Uncertain	0.0090	D
Varity_R	N/A	0.61
VESM-3B	Benign	-8.7

Showing 30 of 30 scores

Splicing Scores

Algorithm	Calibrated pred.	Score	Prediction
DS_DG_spliceai	Uncertain	0.31	Position offset: -2
Pangolin (max)	Benign	0.080
SpliceAI score (max)	Uncertain	0.31	Details are displayed if max score is > 0.2

Showing 3 of 3 scores

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

MaveDB functional evidence

MaveDB is a public repository of laboratory assays that test the effect of thousands of variants at once — treat this as supporting research data and interpret it with great caution; it is not a clinical classification.

No MaveDB functional evidence found for this variant.

Other links and lift over

dbSNP: rs184935465;

hg19: chr19-44169510;

ACMG debug oncogenicity

ACGS debug oncogenicity

ACMG debug germline

Submit to ClinVar